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| Comparison of the copy-neutral loss of heterozygosity identified from whole-exome sequencing data using three different tools |
| Gang-Taik Lee, Yeun-Jun Chung |
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Genomics Inform. 2022;20(1):e4 Published online March 31, 2022 DOI: https://doi.org/10.5808/gi.21066 |
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Comparison of the copy-neutral loss of heterozygosity identified from whole-exome sequencing data using three different tools Genomics & Informatics. 2022;20(1):e4  Whole exome sequencing provides loss of heterozygosity (LoH) data comparable to that of whole genome sequencing (171) Gynecologic Oncology. 2022;166:S100 An evaluation of copy number variation detection tools for cancer using whole exome sequencing data BMC Bioinformatics. 2017;18(1): CLImAT: accurate detection of copy number alteration and loss of heterozygosity in impure and aneuploid tumor samples using whole-genome sequencing data Bioinformatics. 2014;30(18):2576-2583 An Evaluation of Copy Number Variation Detection Tools from Whole-Exome Sequencing Data Human Mutation. 2014;35(7):899-907 Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2 Nucleic Acids Research. 2016;gkw695 Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistan families . 2019; Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families . 2020; Comprehensive Outline of Whole Exome Sequencing Data Analysis Tools Available in Clinical Oncology Cancers. 2019;11(11):1725 A comparison of algorithms for identifying copy number variants in family-based whole-exome sequencing data and its implications in inheritance pattern analysis Gene. 2023;861:147237 |
